United States · FDA National Drug Code directory
misoprostol
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 59762-5008_a2441a04-9c20-452a-91e2-025ad1657568
- Product NDC
- 59762-5008
- Form
- TABLET
- Composition / generic term
- MISOPROSTOL
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20091227
- Source listing expiry
- 20271231
Source-listed ingredients
- MISOPROSTOL — 200 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET in 1 BOTTLE (59762-5008-1) · 59762-5008-1
- 100 TABLET in 1 BOTTLE (59762-5008-2) · 59762-5008-2
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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